The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
127148801 12714880 1 I 20160814 20160824 20160905 20160905 EXP GB-JNJFOC-20160902754 JANSSEN 57.00 YR A F Y 88.90000 KG 20160905 CN GB GB

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
127148801 12714880 1 SS TRAMADOL HYDROCHLORIDE. TRAMADOL HYDROCHLORIDE 1 Oral Y U 283410 0 100 MG UNSPECIFIED
127148801 12714880 2 PS TRAMADOL HYDROCHLORIDE. TRAMADOL HYDROCHLORIDE 1 Oral Y U 283410 20281 50 MG UNSPECIFIED
127148801 12714880 3 C PARACETAMOL ACETAMINOPHEN 1 Unknown U 0 2 DF UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127148801 12714880 1 Sciatica
127148801 12714880 2 Sciatica

Outcome of event

Event ID CASEID OUTC COD
127148801 12714880 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127148801 12714880 Disturbance in attention
127148801 12714880 Dizziness
127148801 12714880 Haemoptysis
127148801 12714880 Hyperhidrosis
127148801 12714880 Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127148801 12714880 2 20160814 20160815 0
127148801 12714880 3 20160815 0